A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094340



Internal ID21277272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:67001841..67005575hg38UCSC Ensembl
Innerchr13:67575973..67579707hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg383735
hg193735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115630
Supporting Variants
Samplessample25
Known GenesPCDH9, PCDH9-AS4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094340
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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